chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 117909079 117909080 A G 1 GENIC homozygous 671772034 1 117909081 117909082 G A 1 GENIC homozygous 671772035 1 117909444 117909445 T TG 10 GENIC heterozygous 769186170 1 117909448 117909449 G - 10 GENIC heterozygous 769186171 1 117909608 117909609 G T 42 GENIC possibly homozygous 671772036 1 117909700 117909701 C CA 28 GENIC homozygous 769186172 1 117910380 117910381 G C 31 GENIC possibly homozygous 671772037 1 117910514 117910516 AT -- 1 GENIC homozygous 769186173 1 117910521 117910522 G GTC 1 GENIC homozygous 769186174 1 117910522 117910523 G GA 1 GENIC homozygous 769186175 1 117910676 117910677 G - 31 GENIC heterozygous 769186176 1 117910715 117910716 C G 27 GENIC heterozygous 671772038 1 117910718 117910719 C T 25 GENIC heterozygous 671772039 1 117910719 117910720 C T 25 GENIC heterozygous 671772040 1 117910719 117910720 C A 25 GENIC heterozygous 671772041 1 117910722 117910723 C G 22 GENIC homozygous 671772042 1 117910730 117910731 T - 19 GENIC heterozygous 769186177 1 117910735 117910736 A G 14 GENIC homozygous 671772043 1 117910935 117910936 G - 37 GENIC heterozygous 769186178 1 117911018 117911019 C CT 49 GENIC possibly homozygous 769186179